Published in Biochim Biophys Acta on October 05, 1972
Interaction of cholera toxin and membrane GM1 ganglioside of small intestine. Proc Natl Acad Sci U S A (1975) 2.18
Ultrastructural localization of cell membrane GM1 ganglioside by cholera toxin. Proc Natl Acad Sci U S A (1977) 1.61
Inhibition of enterotoxin from Escherichia coli and Vibrio cholerae by gangliosides from human milk. Infect Immun (1983) 0.90
Non-collagenous proteins of predentine from dentinogenically active bovine teeth. Biochem J (1983) 0.90
Influenza A virus survival in water is influenced by the origin species of the host cell. Influenza Other Respir Viruses (2013) 0.82
Occurrence of glycosphingolipids in chicken egg yolk. Biochem J (1978) 0.80
Apoptosis of human breast carcinoma cells in the presence of disialosyl gangliosides: II. Treatment of SKBR3 cells with GD3 and GD1b gangliosides. Glycoconj J (2004) 0.80
Molecular cloning and characterization of the expression pattern of the zebrafish alpha2, 8-sialyltransferases (ST8Sia) in the developing nervous system. Glycoconj J (2008) 0.79
Retinal amacrine cell involvement in Tay-Sachs disease. Acta Neuropathol (1981) 0.79
Spinal ganglia and peripheral nerves from a patent with Tay-Sachs disease. Morphological and ganglioside studies. Acta Neuropathol (1985) 0.76
Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure. Proc Natl Acad Sci U S A (1987) 18.91
Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis. Science (1997) 6.66
Identification of HE1 as the second gene of Niemann-Pick C disease. Science (2000) 5.08
Tissue receptor for cholera exotoxin: postulated structure from studies with GM1 ganglioside and related glycolipids. Infect Immun (1973) 4.08
ESPEN Guidelines on Enteral Nutrition: Non-surgical oncology. Clin Nutr (2006) 2.89
A procedure for the quantitative isolation of brain gangliosides. Biochim Biophys Acta (1980) 2.63
The Niemann-Pick C1 protein resides in a vesicular compartment linked to retrograde transport of multiple lysosomal cargo. J Biol Chem (1999) 2.45
A defect in cholesterol esterification in Niemann-Pick disease (type C) patients. Proc Natl Acad Sci U S A (1985) 2.38
Interaction of cholera toxin and membrane GM1 ganglioside of small intestine. Proc Natl Acad Sci U S A (1975) 2.18
Rabbit intestinal glycoprotein receptor for Escherichia coli heat-labile enterotoxin lacking affinity for cholera toxin. Infect Immun (1982) 2.08
A study of finger lengths, semen quality and sex hormones in 360 young men from the general Danish population. Hum Reprod (2005) 1.94
Krabbe disease: a galactosylsphingosine (psychosine) lipidosis. J Lipid Res (1980) 1.93
Fixation and inactivation of cholera toxin by GM1 ganglioside. Scand J Infect Dis (1973) 1.90
Receptor-specific large-scale purification of cholera toxin on silica beads derivatized with lysoGM1 ganglioside. Eur J Biochem (1981) 1.89
The natural history of Niemann-Pick disease type C in the UK. J Inherit Metab Dis (2006) 1.87
Distribution and fatty acid composition of phosphoglycerides in normal human brain. J Lipid Res (1968) 1.83
Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase. Proc Natl Acad Sci U S A (1999) 1.79
Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options. Eur J Neurol (2009) 1.76
Accumulation of glucosylceramide and glucosylsphingosine (psychosine) in cerebrum and cerebellum in infantile and juvenile Gaucher disease. J Neurochem (1982) 1.72
Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids. Hum Mol Genet (1996) 1.70
Somatization in primary care. Prevalence, health care utilization, and general practitioner recognition. Psychosomatics (1999) 1.69
Monoclonal antibodies against gastrointestinal tumour-associated antigens isolated as monosialogangliosides. Int Arch Allergy Appl Immunol (1983) 1.67
Risk factors for intraoperative complications in 1000 extracapsular cataract cases. Ophthalmology (1987) 1.65
A randomized controlled trial of rehabilitation at home after stroke in southwest Stockholm. Stroke (1998) 1.64
A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis. Lancet (1985) 1.64
Ultrastructural localization of cell membrane GM1 ganglioside by cholera toxin. Proc Natl Acad Sci U S A (1977) 1.61
Features of Sjögren's syndrome in patients with primary biliary cirrhosis. J Intern Med (1991) 1.58
Niemann-Pick C disease in Spain: clinical spectrum and development of a disability scale. J Neurol Sci (2006) 1.58
Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype. Am J Hum Genet (1999) 1.57
Type-C Niemann-Pick disease: low density lipoprotein uptake is associated with premature cholesterol accumulation in the Golgi complex and excessive cholesterol storage in lysosomes. Proc Natl Acad Sci U S A (1988) 1.56
Hematopoietic stem-cell transplantation in globoid-cell leukodystrophy. N Engl J Med (1998) 1.47
Growth hormone treatment affects brain neurotransmitters and thyroxine [see comment]. Clin Endocrinol (Oxf) (1996) 1.46
The bone-marrow infiltration pattern in B-cell chronic lymphocytic leukemia is not an important prognostic factor. Danish CLL Study Group. Eur J Haematol (1996) 1.45
Specific gangliosides function as host cell receptors for Sendai virus. Proc Natl Acad Sci U S A (1981) 1.45
Gangliosides and allied glycosphingolipids in human peripheral nerve and spinal cord. Biochim Biophys Acta (1994) 1.44
Absence of hexosaminidase A and B in a normal adult. N Engl J Med (1975) 1.43
Type C Niemann-Pick disease. Abnormal metabolism of low density lipoprotein in homozygous and heterozygous fibroblasts. J Biol Chem (1986) 1.41
Cerebrospinal fluid monoamine metabolites and atmospheric pressure. Biol Psychiatry (1996) 1.39
Niemann-Pick disease type C: spectrum of HE1 mutations and genotype/phenotype correlations in the NPC2 group. Am J Hum Genet (2001) 1.38
A double-blind evaluation of electroconvulsive therapy in Parkinson's disease with "on-off" phenomena. Acta Neurol Scand (1987) 1.36
Acid sphingomyelinase deficiency. Phenotype variability with prevalence of intermediate phenotype in a series of twenty-five Czech and Slovak patients. A multi-approach study. J Inherit Metab Dis (2005) 1.36
Niemann-Pick C1 disease: correlations between NPC1 mutations, levels of NPC1 protein, and phenotypes emphasize the functional significance of the putative sterol-sensing domain and of the cysteine-rich luminal loop. Am J Hum Genet (2001) 1.34
Human brain gangliosides: developmental changes from early fetal stage to advanced age. Biochim Biophys Acta (1989) 1.34
Linkage of Niemann-Pick disease type C to human chromosome 18. Proc Natl Acad Sci U S A (1993) 1.33
Immunological and catalytic quantitation of splenic glucocerebrosidase from the three clinical forms of Gaucher disease. Am J Hum Genet (1983) 1.33
Detection by monoclonal antibody of carbohydrate antigen CA 50 in serum of patients with carcinoma. Br Med J (Clin Res Ed) (1984) 1.31
Blood-brain barrier disturbance in patients with Alzheimer's disease is related to vascular factors. Acta Neurol Scand (1990) 1.29
Peripheral and central hypomyelination with hypogonadotropic hypogonadism and hypodontia. Neurology (2006) 1.28
Sendai virus receptor: proposed recognition structure based on binding to plastic-adsorbed gangliosides. Proc Natl Acad Sci U S A (1980) 1.27
Type C Niemann-Pick disease. A parallel loss of regulatory responses in both the uptake and esterification of low density lipoprotein-derived cholesterol in cultured fibroblasts. J Biol Chem (1986) 1.27
Pulmonary arteriovenous fistulas in hereditary hemorrhagic telangiectasia. Acta Med Scand (1985) 1.27
Sialosyllactotetraosylceramide, a novel ganglioside antigen detected in human carcinomas by a monoclonal antibody. FEBS Lett (1985) 1.26
Biochemical studies in Niemann-Pick disease. I. Major sphingolipids of liver and spleen. Biochim Biophys Acta (1983) 1.25
Structure of the major glucosamine-containing ganglioside of human tissues. J Biol Chem (1973) 1.25
Generalized CNS disease and massive GM1-ganglioside accumulation in mice defective in lysosomal acid beta-galactosidase. Hum Mol Genet (1997) 1.24
The steroidogenic acute regulatory protein homolog MLN64, a late endosomal cholesterol-binding protein. J Biol Chem (2000) 1.23
NPC1 gene mutations in Japanese patients with Niemann-Pick disease type C. Hum Genet (1999) 1.23
Screening for somatization and hypochondriasis in primary care and neurological in-patients: a seven-item scale for hypochondriasis and somatization. J Psychosom Res (1999) 1.23
Genetic heterogeneity in Gaucher disease: physicokinetic and immunologic studies of the residual enzyme in cultured fibroblasts from non-neuronopathic and neuronopathic patients. Am J Med Genet (1985) 1.21
The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation. Am J Hum Genet (2000) 1.19
Polystyrene-adsorbed gangliosides for investigation of the structure of the tetanus-toxin receptor. Eur J Biochem (1980) 1.19
Niemann-Pick C disease: functional characterization of three NPC2 mutations and clinical and molecular update on patients with NPC2. Clin Genet (2007) 1.18
A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse. Hum Mol Genet (2001) 1.18
Changes in the fatty acid composition of cerebrosides and sulfatides of human nervous tissue with age. J Lipid Res (1968) 1.17
Depletion of rafts in late endocytic membranes is controlled by NPC1-dependent recycling of cholesterol to the plasma membrane. J Cell Sci (2001) 1.17
Developmental profiles of gangliosides in human and rat brain. J Neurochem (1971) 1.17
Comparison of receptors for cholera and Escherichia coli enterotoxins in human intestine. Gastroenterology (1985) 1.17
Calcium/calmodulin inhibition of basic-helix-loop-helix transcription factor domains. Nature (1994) 1.15
Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouse. Hum Mol Genet (2000) 1.14
Neuropathology of the Norrbottnian type of Gaucher disease. Morphological and biochemical studies. Acta Neuropathol (1984) 1.14
Protein analysis in cerebrospinal fluid. II. Reference values derived from healthy individuals 18-88 years of age. Eur Neurol (1993) 1.13
Chemical structure of carcinoma ganglioside antigens defined by monoclonal antibody C-50 and some allied gangliosides of human pancreatic adenocarcinoma. Biochim Biophys Acta (1985) 1.13
The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterol. Biochim Biophys Acta (1994) 1.12
Splenic transplantation in a case of Gaucher's disease. Lancet (1971) 1.12
Sphingosylphosphorylcholine in Niemann-Pick disease brain: accumulation in type A but not in type B. Neurochem Res (1999) 1.10
A sulfated glucosylceramide from rat kidney. J Biol Chem (1989) 1.10
Niemann-Pick type C disease: NPC1 mutations associated with severe and mild cellular cholesterol trafficking alterations. Hum Genet (2001) 1.10
Identification of 25 new mutations in 40 unrelated Spanish Niemann-Pick type C patients: genotype-phenotype correlations. Clin Genet (2005) 1.09
Deleted ring chromosome 22 in a mentally retarded boy. Clin Genet (1986) 1.09
Type C Niemann-Pick disease: use of hydrophobic amines to study defective cholesterol transport. Dev Neurosci (1991) 1.08
Separation of gangliosides on a new type of anion-exchange resin. Biochim Biophys Acta (1980) 1.08
Gangliosides as receptors for bacterial toxins and Sendai virus. Adv Exp Med Biol (1980) 1.07
Ten years' experience of bone marrow transplantation for Gaucher disease. Transplantation (1995) 1.07
Seasonal and circadian monoamine variations in human brains examined post mortem. Acta Psychiatr Scand Suppl (1980) 1.07
Receptor ganglioside content of three hosts for Sendai virus. MDBK, HeLa, and MDCK cells. Biochim Biophys Acta (1984) 1.06
Isolation and structural determination of a novel ganglioside, a disialosylpentahexosylceramide from human brain. J Biol Chem (1973) 1.06
Blood brain barrier function in vascular dementia. Acta Neurol Scand (1990) 1.06
Characterization of the binding epitope of a monoclonal antibody to sulphatide. Biochem J (1988) 1.05
Free sphingoid bases in tissues from patients with type C Niemann-Pick disease and other lysosomal storage disorders. Biochim Biophys Acta (1994) 1.04